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  • What: Brief presentations on topics such as IRB Updates, Clinical Trial Recruitment, Clinical Trial Billing, Best Budget Practices, Informed Consenting, HIPAA Regulations, and more!
  • Why: The goal of this program is to fill any gaps in information related to the implementation of clinical trials that have been identified by investigators and their research teams.
  • When: Offered the first and third Thursday of each month. Usually from 12:00-1:00pm.
  • Who: Seminar topics will be of interest and relevance to clinical research personnel including investigators, regulatory personnel, study coordinators and financial administrators. *CME credits provided for each session